Evidence map›Paper›PMID 32011097›Full record

ReviewChemistry, an Asian journal2020

Carbometalation and Heterometalation of Carbon-Carbon Multiple-Bonds Using Group-13 Heavy Metals: Carbogallation, Carboindation, Heterogallation, and Heteroindation.

Yoshihiro Nishimoto, Makoto Yasuda

Abstract readReview
In one paragraph

Review in Chemistry, an Asian journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Yoshihiro NishimotoDepartment of Applied Chemistry Graduate School of Engineering, Osaka University 2-1 Yamadaoka, Suita, 565-0871, Osaka, Japan.
Makoto YasudaDepartment of Applied Chemistry Graduate School of Engineering, Osaka University 2-1 Yamadaoka, Suita, 565-0871, Osaka, Japan.ORCID http://orcid.org/0000-0002-6618-2893

Funding

Frontier Research Base for Global Young Researchers, Osaka UniversityJSPS KAKENHI JP15H05848Middle Molecular Strategy JP16 K05719Middle Molecular Strategy JP18H01977Middle Molecular Strategy JP18 K19079Middle Molecular Strategy JP19 K05455
6 · The paper itself

Abstract

Organogallium and -indium compounds are useful reagents in organic synthesis because of their moderate stability, efficient reactivity and high chemoselectivity. Carbogallation and -indation of a carbon-carbon multiple bond achieves the simultaneous formation of carbon-carbon and carbon-metal bonds. Heterogallation and -indation construct carbon-heteroatom and carbon-metal bonds. Therefore, these reaction systems represent a significant synthetic method for organogalliums and -indiums. Many chemists have attempted to apply various types of unsaturated compounds such as alkynes, alkenes, and allenes to these reaction systems. This minireview provides an overview of carboindation and -gallation as well as heteroindation and -gallation.

Indexed as

CarbometalationGalliumHeterometalationIndiumMetalation

Identifiers

PMID32011097
PMCPMC7155119

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.